Reported Dec 4, 2024 · Ongoing
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482S; use in Peritoneal Dialysis
Baxter Healthcare Corporation
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Baxter Healthcare Corporation · 1 Baxter Pkwy · Deerfield, IL · 60015-4625
Is this the product you have?
- Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482S; use in Peritoneal Dialysis
- Lot codes and dates
- UDI/DI 00085412476261
- Lot/Serial Numbers
H23J13063H23J26081H24B18059H24B19065H24B19099H24B20071H24C18065H24E22062H24F11048
- Amount recalled
- 31248 units
This recall covers 11 products
The agency filed one notice per product. You are reading one of them; the other 10 are below.
Why it was recalled
There has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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